2-Amino-4-bromo-3-methylbenzoic acid
95%
- Product Code: 64228
CAS:
129833-29-0
| Molecular Weight: | 230.06 g./mol | Molecular Formula: | C₈H₈BrNO₂ |
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| EC Number: | MDL Number: | MFCD17244230 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, avoid light, store in inert gas |
Product Description:
This chemical is primarily used in organic synthesis as a building block for more complex compounds. It serves as an intermediate in the production of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that target specific diseases. Its structure, featuring both amino and carboxylic acid functional groups, makes it versatile for coupling reactions, enabling the creation of diverse molecular frameworks. Additionally, it is employed in the synthesis of agrochemicals, where it contributes to the development of herbicides or pesticides. The bromine atom in its structure allows for further functionalization through substitution reactions, enhancing its utility in fine chemical manufacturing. Researchers also utilize it in the study of structure-activity relationships (SAR) to optimize the efficacy of drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,377.00 |
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| 0.250 | 10-20 days | ฿2,070.00 |
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| 1.000 | 10-20 days | ฿5,175.00 |
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2-Amino-4-bromo-3-methylbenzoic acid
This chemical is primarily used in organic synthesis as a building block for more complex compounds. It serves as an intermediate in the production of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that target specific diseases. Its structure, featuring both amino and carboxylic acid functional groups, makes it versatile for coupling reactions, enabling the creation of diverse molecular frameworks. Additionally, it is employed in the synthesis of agrochemicals, where it contributes to the development of herbicides or pesticides. The bromine atom in its structure allows for further functionalization through substitution reactions, enhancing its utility in fine chemical manufacturing. Researchers also utilize it in the study of structure-activity relationships (SAR) to optimize the efficacy of drug candidates.
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